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LMA North America Recalls

1 recall on record · July 25, 2012 to July 25, 2012 · Medical Devices

July 25, 2012Medical DevicesFDA

LMA North America Inc recalls LMA Esophageal Intubation Detector (EID), Catalog Number EID100 The device is used to assist verification of placemen

Hazard: The recall was initiated because LMANA has received a complaint that the Esophageal Intubation Detector (EID100) has a potential to create a false positive if used on a patient during confirmation of intubation.

LMA North America Recalls | RecallWatchUSA